• Title/Summary/Keyword: tailing analysis

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Structural Transcription of Organogels to Mesoporous Silicas: A Chain-length Dependent Morphology and Pore Texture

  • Huang, Yaqun
    • Bulletin of the Korean Chemical Society
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    • v.33 no.11
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    • pp.3711-3718
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    • 2012
  • Here, we report a chain-length dependent morphology and pore structure tailing of mesoporous silica templated from organogels, which is formed by primary alkylamine and ethylene glycol at room temperature. As the chain length of alkylamine changes from 12 to 18, the resulted materials exhibit a morphology change from layers to spheres and platelets, respectively. SEM and TEM observation revealed that these shapes appear to be inherited from their parent organogels. Further pore structure characterization by nitrogen sorption analysis demonstrates that all the resulted silicas exhibit typical IV isotherms indicative of uniform mesopores, and their pore sizes are dependent on the chain length of alkylamine used.

Analysis of Hydrodynamic Dispersion in Contaminated Soil based on Mobile-Immobile Model (Mobile-Immobile 모델을 활용한 유류오염토양 내 수리분산 특성 연구)

  • Kim, Yong-Sung;Woo, Hee-Soo;Park, Jun-Boum
    • Proceedings of the Korean Geotechical Society Conference
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    • 2008.10a
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    • pp.1512-1517
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    • 2008
  • Laboratory column tests were conducted in this study using $Cl^-$ tracers on Jumunjin sand to analyze contaminant transport in mixed contaminated soils. Results obtained from clean soils and soils containing residual diesel verified heterogeneous distribution of residual diesel, and clear acceleration of solute movement. In addition, asymmetric breakthrough curves indicated development of immobile region where solute movement becomes stagnant and creates tailing phenomenon.

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Analysis of mine tailings, field soils, and paddy soils around Jingok abandoned mine (진곡광산 광미와 주변 토양의 오염조사)

  • 김선태;윤양희;박제안;심의섭
    • Journal of Korea Soil Environment Society
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    • v.4 no.2
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    • pp.175-183
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    • 1999
  • Mine tailings, field soils, and paddy soils around Jingok abandoned mine were analyzed In order to investigate their pollution levels of heavy metals and cyanide. The average contents of As, Cd, Cu. Hg. Pb, Zn, and CN ̄in mine tailings were 3.94$\times$$10^3$, 14.3, 266, 6.13, 4.07$\times$$10^3$, 2.51$\times$$10^3$, and 1.19mg/kg, respectively. The pollution indices calculated by the tolerance level of Kloke were 32~58 and the pH values were slightly acidic in mine tailings. In the field and paddy soils of Jingok abandoned mine area except for soils nearby mine tailings, concentrations of the heavy metals were less than standards of soil pollution of agricultural area in the environmental protection law.

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FEM Analysis on Rolling Contact Fatigue Crack of a Railway Wheel (철도 차륜의 구름접촉 피로 균열에 관한 유한요소해석)

  • Kim, Ho-Kyung;Yang, Kyoung-Tak;Kim, Hyun-Jun
    • Journal of the Korean Society of Safety
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    • v.22 no.2 s.80
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    • pp.8-14
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    • 2007
  • In this study, tensile and fatigue crack propagation tests machined from actual wheels were performed. FEM analysis also was performed on the crack that was assumed to be 15 mm in depth under the wheel tread surface. The stress intensity factors K I and K II at the crack tip under the stress($P_{max}=911.5MPa$) due to a rolling contact were analyzed for crack growth characteristics. As a result, the perpendicular crack was found to be more dangerous compared to the parallel one. It is found that in the wheel fatigue crack, parallel to the wheel tread surface, the crack with its length 2a = 2.4mm starts to propagate due to the fact that the effective stress intensity factor access to the threshold stress intensity factor($K_{th}=16.04MPa{\sqrt{m}}$) of the wheel.

Distribution of heavy metals and cyanide in tailings, soils, and stream sediments around Gubong disused mine (구봉광산 주변 토양에서의 중금속과 시안의 분포)

  • 김선태;윤양희;박제안;심의섭
    • Journal of Korea Soil Environment Society
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    • v.4 no.1
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    • pp.35-47
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    • 1999
  • Mine tailings, soils. stream sediments around Gubong disused mine were analyzed in order to investigate their distribution and pollution levels of heavy metals and cyanide. The average contents of As, Cd, Cu. Hg, Pb, Zn, and CN ̄ in mine tailings were 6.93$\times$$10^{3}$, 56.9, 209, 5.03, 3.25$\times$$10^{3}$, 1.89$\times$$10^{3}$, 21mg/kg respectively. The pollution indices that calculated by the tolerance level of Kloke were 42~95 and the pH values were slightly alkaline in mine tailings. The contents of heavy metals and cyanide in field soils near the mine were higher than the paddy soils. The contents of heavy metals in the stream sediment were up to that of the tailings, so contamination from the mine tailings were serious.

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Soil Samples in 134Cs of the 604, 795 keV Spectrum Analysis (토양시료 속 134Cs의 604, 795 keV 에너지 스펙트럼 분석)

  • Jang, Eunsung
    • Journal of the Korean Society of Radiology
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    • v.8 no.7
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    • pp.443-447
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    • 2014
  • $^{134}Cs$ radioactive concentration among soil samples is difficult to classify due to the background impact on crust originated natural radioactive nuclide, and overlapping and interfering between peaks. The ways to identify true peaks in gamma-ray spectroscopy are as follows to reduce statistical fluctuation by smoothing based on the fact that the shapes of peak are mostly Gaussian, to inspect the levels of width and height of peaks, to add functions on low-energy trailing phenomena, or 4) to check the peaks after modifying Gaussian function itself. Therefore, it is considered that information and knowledge for spectrum analysis are necessary.

The analysis of Bismuth metal and its alloy by using of cation exchanger (양이온교환수지에 의한 비스무트 지금 및 합금의 분리 정량)

  • Myon-young Park;Byong-Cho Lee;Kee-Chae Park
    • Journal of the Korean Chemical Society
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    • v.15 no.2
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    • pp.49-54
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    • 1971
  • It is shown that the impurities of Cu(II), Pb(II), Zn(II) and Ag(I) in Bismuth metal and the components of Pb(II), Zn(II) and Sn(IV) in Bismuth alloy are separated into their components from each other by elutions through $3.14cm^2{\times}10cm$ cation exchange resin, $Dowex\;50w\;{\times}\;8$ (100~200 mesh), column with the mixed solutions of HAc and NaAc as the eluents. The elution curve of Fe(III) has a long tailing and is not separated quantitatively from Bi(III). The eluents used for this separation are as follows; 1M HAc + 0.1M NaAc (pH 3.36) for Fe(III) and Bi (III). 0.3M HAc + 0.3M NaAc (pH 4.70) for Cu(II), Pb(II) and Zn(II). 0.5M HAc + 0.5M NaAc (pH4.70) for Ag(I) and Sn(IV). The analysis of cations eluted are carried out by spectrophotometry and EDTA titrimetry. Their recoveries are more than 99%.

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Analytical Quality by Design Methodology Approach for Simultaneous Quantitation of Paeoniflorin and Decursin in Herbal Medicine by RP-HPLC Analysis

  • Kim, Min Kyoung;Park, Geonha;Hong, Seon-Pyo;Jang, Young Pyo
    • Natural Product Sciences
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    • v.27 no.4
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    • pp.264-273
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    • 2021
  • Simultaneous quantification of multiple marker compounds in herbal medicine by high performance liquid chromatography (HPLC) analysis is still a challenge due to the complexity in various parameters to be considered and co-existing multi-components. As a case study, a reliable HPLC method for simultaneous quantification of paeoniflorin from Paeoniae Radix and decursin from Angelicae Gigantis Radix in various commercial herbal medicine was developed based on analytical quality by design (AQbD) strategy. As a first step, risk assessment was performed to select the critical method parameters (CMPs) which were decided as organic mobile phase ratio and column oven temperature. In order to evaluate the effect of the CMPs on critical method attributes (CMAs) of peak resolution and tailing, central composite design (CCD) was employed. The final chromatographic conditions were optimized as follows: column- C18, 4.6 × 250 mm, 5 ㎛ particle size; mobile phase- A: acetonitrile, B: 0.1% acetic acid water; detection wavelength- 235 nm for paeoniflorin, 325 nm for decursin; column oven temperature- 25℃; flow rate- 1.0 mL/min; gradient mobile phase system as Time (min) : % A, 0:14, 25:14, 30:50, 60:50, 61:100, 65:100, 66:14, 75:14. The method was successfully validated according to the International Conference on Harmonization (ICH) guidelines and piloted for ten commercial herbal medicines.

Determination of Thiamine in Pharmaceutical Preparations by Reverse Phase Liquid Chromatography Without Use of Organic Solvent

  • Suh, Joon Hyuk;Kim, Junghyun;Jung, Juhee;Kim, Kyunghyun;Lee, Seul Gi;Cho, Hyun-Deok;Jung, Yura;Han, Sang Beom
    • Bulletin of the Korean Chemical Society
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    • v.34 no.6
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    • pp.1745-1750
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    • 2013
  • A novel green aqueous mobile phase modified with room temperature ionic liquids (RTILs) was employed in the absence of volatile organic solvents or ion-pairing reagents to analyze thiamine, a very polar compound, by reverse phase high performance liquid chromatography (RP-HPLC). Due to its strongly hydrophilic nature, thiamine was eluted near the column dead time ($t_0$) using a mobile phase without adding RTILs or ion-pairing reagents, even if a 100% aqueous mobile phase, which has weak elution power under reverse phase conditions, was used. Thus, 1-ethyl-3-methyl-imidazolium hexafluorophosphate ([EMIM][$PF_6$]), which has the strongest chaotropic effect, was selected as a mobile phase additive to improve retention and avoid baseline disturbances at $t_0$. Various mobile phase parameters such as cation moiety, chaotropic anion moiety, pH and concentration of RTILs were optimized to determine thiamine at the proper retention time. Method validation was performed to assess linearity, intra- and inter-day accuracy and precision, recovery and repeatability; all results were found to be satisfactory. The developed method was also compared to the current official United States Pharmacopoeia (USP) and Korean Pharmacopoeia (KP) methods using an organic mobile phase containing an ionpairing reagent by means of evaluating various chromatographic parameters such as the capacity factor, theoretical plate number, peak asymmetry and tailing factor. The results indicated that the proposed method exhibited better efficiency of thiamine analysis than the official methods, and it was successfully applied to quantify thiamine in pharmaceutical preparations.

A Study on Chemical Compositions of Sediment and Surface Water in Nakdong River for Tracing Contaminants from Mining Activities (광해오염원 추적을 위한 낙동강 지역 퇴적물 및 하천수의 화학조성 연구)

  • Kim, Jiyun;Choi, Uikyu;Baek, Seung-Han;Choi, Hye-Bin;Lee, Jeonghoon
    • Journal of the Korean earth science society
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    • v.37 no.4
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    • pp.211-217
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    • 2016
  • There have been found mine tailings, wastes, and mining drainage scattered in the area of Nakdong River due to the improper maintenance of the abandoned mines. These contaminants can flow into rivers during the heavy rain periods in summer. Along the study area beginning Seokpo-myeon, Bonghwa-gun of Gyeongsangbuk-do untill Dosan-myeon, Andong-si, there are one hundred five mines including sixty metalliferous mines and forty-five nonmetal mines, which can adversely affect the adjacent rivers. To verify the contamination, we collected sediments, seepage water and surface water for a year both in rainy season and dry season. This study found that sediments, containing high concentrations of heavy metals caused by mining activities, are dispersed throughout the entire river basin (68 sample points with pollution index, based on the concentration of trace element, (PI) >10 among the total of 101 samples). The results of river water analysis indicated the increased concentrations of arsenic and cadmium at branches from Seungbu, Sambo, Okbang and Janggun mine, which concerns that the river water may be contaminated by mining drainage and tailing sediments. However, it is difficult to sort out the exact sources of contamination in sediments and waters only by using the chemical compositions. Thus the control of mining pollution is challenging. To prevent water from being contaminated by mining activities, we should be able to divide inflow rates from each origin of the mines. Therefore, there should be a continued study about how to trace the source of contaminants from mining activities by analyzing stable isotopes.